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临床试验/CTRI/2019/10/021735
CTRI/2019/10/021735尚未招募1 期

Effect of pre-operative vaginal preparation with Povidone Iodine before abdominal hysterectomy at AIIMS Rishikesh: A Randomised Controlled Trial

AIIMS Rishikesh1 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2019年10月25日最近更新:
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试验速览

阶段
1 期
状态
尚未招募
入组人数
150
试验地点
1
主要终点
post operative infections
研究概览研究设计入排标准结局指标研究者研究点记录与标识符相似试验

研究概览

简要总结

To study the  effect of vaginal preparation on post operative infectious morbidity to determine its usefulness considering the practice of omitting this practice at many centres including our institute due to lack of sufficient evidences supporting this routine

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Participant Blinded

入排标准

年龄范围
14.00 Year(s) 至 65.00 Year(s)（—）
性别
Female

入选标准

  • •reproductive age females.

排除标准

  • •1.Patients undergoing vaginal hysterectomy 2.Patients undergoing laparoscopic hysterectomy 3Patients undergoing emergency hysterectomy 4.Patients undergoing obstetric hysterectomy 5.Patients allergic to iodine containing solutions.
  • •6.Patients undergoing hysterectomies for malignant indications.

结局指标

主要结局

post operative infections

时间窗: 48 hours, 8 days,4 weeks

次要结局

  • comparing the types of post operative infections in two groups(day 2, 8, 4 weeks post op)

研究者

申办方类型
Research institution and hospital

研究点 (1)

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